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Beijing: Chinese Herbal Pieces enterprises to apply tampering test results re-treatment

  Recently, the Beijing Municipal Food and Drug Administration issued "on the further strengthening of production supervision of Chinese medicine Pieces notice", requiring Chinese Herbal Pieces of internal response to Chinese herbal medicines, excipients and drug packaging materials to implement batch management, to achieve tracking by batch number, crack down on undocumented , Ultra-range production and sales of Chinese medicine Pieces. The GMP Certificate for Pharmaceuticals shall be withdrawn as serious defects in the GMP of drugs which have been seriously dealt with according to the law and are seriously dealt with according to the law if the test results or data are falsely used or tampered with or used in accordance with the inspection rules.

  The notice clearly, in the approved "drug production license", "Drug GMP certificate" in the venue, facilities, equipment, without approval shall not engage in research and production, sales of unrelated behavior. Strengthen the Chinese herbal medicines, processed materials and drug packaging materials, traceability management, Pieces of Chinese medicine production enterprises must be strictly in accordance with the relevant requirements of pharmaceutical GMP and the variety of production process rules, the whole process must be completed in the approved plant, batch production records should be timely, True and complete record of the processing process.

  Notice requirements, Beijing District Council, directly under the branch should be the production of Chinese medicine Pieces into key regulatory areas, the flight inspection and spot checks as a routine means of supervision. According to the law strictly investigate and deal with the production of Chinese medicine Pieces of illegal acts.